一些新的噻唑取代的1,3,4-恶二唑衍生物的合成及抗菌筛选

ECSOC-25 Pub Date : 2021-11-15 DOI:10.3390/ecsoc-25-11662
Siddhant V. Kokate, S. Patil
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引用次数: 0

摘要

本文研究了新型噻唑取代的1,3,4-恶二唑衍生物的合成及其抑菌活性。不同的硫酰胺与4-氯-3-氧丁酸乙酯(4-氯乙基乙酰乙酸酯)反应得到2-(2-芳基噻唑-4-基)乙酸乙酯,与水合肼在无水乙醇中反应得到2-(2-芳基噻唑-4-基)乙酰吡嗪。2-(2-芳基噻唑-4-基)乙酰肼在乙醇水溶液中与cs2和KOH反应生成5-((2-芳基噻唑-4-基)甲基)-1,3,4-恶二唑-2-硫醇。最后,在室温下用α -环酮进一步处理5-((2-芳基噻唑-4-基)甲基)-1,3,4-恶二唑-2-硫醇,得到目标化合物。大多数化合物具有良好的抗菌和抗真菌活性。4-chloro-3-oxobuta-noate;α -环酮;抗菌和抗真菌活性
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Synthesis and Antimicrobial Screening of Some New Thiazole Substituted 1,3,4-Oxadiazole Derivatives
: In the present work the synthesis and antimicrobial activity of new thiazole substituted 1,3,4-oxadiazole derivatives was achieved. The reaction of different thioamides with ethyl 4-chloro-3-oxobutanoate (4-chloro ethyl acetoacetate) gave ethyl 2(2-arylthiazol-4yl)acetate , which on subse-quent reaction with hydrazine hydrate in absolute ethanol afforded 2-(2-arylthiazol-4-yl)acetohy-drazide. 2-(2-arylthiazol-4-yl) acetohydrazide on reaction with CS 2 and KOH in aqueous ethanol cyclized to form 5-((2-arylthiazol-4-yl)methyl)-1,3,4-oxadiazole-2-thiol. Finally, 5-((2-arylthiazol-4-yl) methyl)-1,3,4-oxadiazole-2-thiol were further treated with α -halo ketones at room temperature to afford the target compounds . Most of the compounds showed good antibacterial as well as antifungal activity. 4-chloro-3-oxobuta-noate; α -halo ketones; antibacterial and antifungal activity
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